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3 in total

1. AXILLARY FRECKLING AS A DIAGNOSTIC AID IN NEUROFIBROMATOSIS.

Authors: F W CROWE
Journal: Ann Intern Med Date: 1964-12 Impact factor: 25.391

2. Diagnostic importance of café-au-lait spot in neurofibromatosis.

Authors: F W CROWE; W J SCHULL
Journal: AMA Arch Intern Med Date: 1953-06

3. Diagnostic value of the café-au-lait spot in children.

Authors: D Whitehouse
Journal: Arch Dis Child Date: 1966-06 Impact factor: 3.791

3 in total

22 in total

1. Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis).

Authors: B D Coppin; I K Temple
Journal: J Med Genet Date: 1997-07 Impact factor: 6.318

2. Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.

Authors: M Sharland; R Taylor; M A Patton; S Jeffery
Journal: J Med Genet Date: 1992-03 Impact factor: 6.318

3. Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome.

Authors: C J van Asperen; W C Overweg-Plandsoen; M H Cnossen; D A van Tijn; R C Hennekam
Journal: J Med Genet Date: 1998-04 Impact factor: 6.318

4. Cardiovascular malformations and the neural crest.

Authors: J B Beckwith
Journal: Pediatr Radiol Date: 1989

5. The heart in lentiginosis.

Authors: J Somerville; R E Bonham-Carter
Journal: Br Heart J Date: 1972-01

6. Progressive cardiomyopathic lentiginosis: first report of autopsy findings in a recently recognized inheritable disorder (Autosomal dominant).

Authors: E J Moynahan
Journal: Proc R Soc Med Date: 1970-05

7. [Electrocardiographic examination in patients with skin diseases].

Authors: R Denk
Journal: Arch Kreislaufforsch Date: 1969-10

8. Profuse lentiginosis, minor cardiac abnormality, and small stature.

Authors: D C Macmillan; H R Vickers
Journal: Proc R Soc Med Date: 1969-10

Review 9. Molecular genetics of neurofibromatosis type 1 (NF1).

Authors: M H Shen; P S Harper; M Upadhyaya
Journal: J Med Genet Date: 1996-01 Impact factor: 6.318

10. Increased rate of missense/in-frame mutations in individuals with NF1-related pulmonary stenosis: a novel genotype-phenotype correlation.

Authors: Shay Ben-Shachar; Shlomi Constantini; Hen Hallevi; Emma K Sach; Meena Upadhyaya; Gareth D Evans; Susan M Huson
Journal: Eur J Hum Genet Date: 2012-10-10 Impact factor: 4.246